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代谢功能障碍相关脂肪性肝病比非酒精性脂肪性肝病表现出更多的肝纤维化。

Metabolic dysfunction-associated fatty liver disease indicates more hepatic fibrosis than nonalcoholic fatty liver disease.

作者信息

Hong Shan, Hong Zifan, Hao Yiwei, Sun Lei, Wei Hongshan

机构信息

Department of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.

Department of Applied Information, Tomsk State University, Tomsk, Russia.

出版信息

Medicine (Baltimore). 2025 Feb 7;104(6):e41455. doi: 10.1097/MD.0000000000041455.


DOI:10.1097/MD.0000000000041455
PMID:39928810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11813007/
Abstract

The term metabolic dysfunction-associated fatty liver disease (MAFLD) has been proposed based on a redefinition of the nonalcoholic fatty liver disease (NAFLD) criteria. Our study aimed to address the knowledge gap by comparing the diagnostic accuracy of MAFLD and NAFLD criteria in identifying significant fibrosis among patients with hepatic steatosis. A cross-sectional study was conducted on 2626 patients with hepatic steatosis treated at Beijing Ditan Hospital between January 2009 and December 2022. Patients with viral hepatitis were excluded. Significant fibrosis was defined as a Meta-analysis of Histological Data in Viral Hepatitis (METAVIR) score F ≥ 2. MAFLD and NAFLD were diagnosed in 478 and 428 patients, respectively. Clinicopathological characteristics were compared between the MAFLD+ NAFLD- group (patients who met the criteria for MAFLD but not NAFLD) and MAFLD- NAFLD+ group (patients who met the criteria for NAFLD but not MAFLD). A total of 743 patients with histologically verified hepatic steatosis were analyzed. The MAFLD+ NAFLD- group comprised 163 (21.9%) and the MAFLD- NAFLD+ group comprised 113 (15.2%) patients. Patients in the MAFLD+ NAFLD- group were older and more likely to be male and had higher body mass index and liver stiffness levels than those in the MAFLD- NAFLD+ group. The prevalence of significant fibrosis was higher in the MAFLD+ NAFLD- group than in the MAFLD- NAFLD+ group (43.6% vs 15.9%, P < .001). The MAFLD criteria may be a better indicator of fibrosis than the NAFLD criteria. Fibrosis in patients with MAFLD can be determined by metabolic disorders, not excessive alcohol consumption.

摘要

代谢功能障碍相关脂肪性肝病(MAFLD)这一术语是基于对非酒精性脂肪性肝病(NAFLD)标准的重新定义而提出的。我们的研究旨在通过比较MAFLD和NAFLD标准在识别肝脂肪变性患者显著纤维化方面的诊断准确性来填补知识空白。对2009年1月至2022年12月在北京地坛医院接受治疗的2626例肝脂肪变性患者进行了一项横断面研究。排除病毒性肝炎患者。显著纤维化定义为病毒性肝炎组织学数据的Meta分析(METAVIR)评分F≥2。分别有478例和428例患者被诊断为MAFLD和NAFLD。比较了MAFLD+NAFLD-组(符合MAFLD标准但不符合NAFLD标准的患者)和MAFLD-NAFLD+组(符合NAFLD标准但不符合MAFLD标准的患者)的临床病理特征。对743例经组织学证实为肝脂肪变性的患者进行了分析。MAFLD+NAFLD-组包括163例(21.9%)患者,MAFLD-NAFLD+组包括113例(15.2%)患者。MAFLD+NAFLD-组的患者年龄更大,男性比例更高,体重指数和肝脏硬度水平高于MAFLD-NAFLD+组。MAFLD+NAFLD-组显著纤维化的患病率高于MAFLD-NAFLD+组(43.6%对15.9%,P<0.001)。MAFLD标准可能比NAFLD标准更能准确指示纤维化。MAFLD患者的纤维化可由代谢紊乱决定,而非过量饮酒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/d3c310869763/medi-104-e41455-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/973619d5550e/medi-104-e41455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/54245c22ba5c/medi-104-e41455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/d3c310869763/medi-104-e41455-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/973619d5550e/medi-104-e41455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/54245c22ba5c/medi-104-e41455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7556/11813007/d3c310869763/medi-104-e41455-g003.jpg

相似文献

[1]
Metabolic dysfunction-associated fatty liver disease indicates more hepatic fibrosis than nonalcoholic fatty liver disease.

Medicine (Baltimore). 2025-2-7

[2]
Comparative application of MAFLD and MASLD diagnostic criteria on NAFLD patients: insights from a single-center cohort.

Clin Exp Med. 2025-1-14

[3]
Metabolic dysfunction-associated fatty liver disease and nonalcoholic fatty liver disease from clinical to pathological characteristics: a multi-center cross-sectional study in real world.

Postgrad Med J. 2024-4-22

[4]
Metabolic dysfunction-associated fatty liver disease improves detection of high liver stiffness: The Rotterdam Study.

Hepatology. 2022-2

[5]
Fibrosis-4 Index Score Predicts Concomitant Coronary Artery Diseases Across the Spectrum of Fatty Liver Disease.

Dig Dis Sci. 2023-9

[6]
MAFLD identifies patients with significant hepatic fibrosis better than NAFLD.

Liver Int. 2020-12

[7]
The impact of concomitant hepatitis C virus infection on liver and cardiovascular risks in patients with metabolic-associated fatty liver disease.

Eur J Gastroenterol Hepatol. 2023-11-1

[8]
Impact of nomenclature as metabolic associated steatotic liver disease on steatotic liver disease prevalence and screening: a prospective population survey in Asians.

J Gastroenterol Hepatol. 2024-8

[9]
Clinical and Histologic Features of Patients with Biopsy-Proven Metabolic Dysfunction-Associated Fatty Liver Disease.

Gut Liver. 2021-5-15

[10]
Elevated concurrent carotid atherosclerosis rates in patients with metabolic dysfunction-associated fatty liver disease (MAFLD) compared to non-alcoholic fatty liver disease (NAFLD): A cross-sectional observational study.

Nutr Metab Cardiovasc Dis. 2025-1

本文引用的文献

[1]
Comparison of NAFLD, MAFLD, and MASLD Prevalence and Clinical Characteristics in Asia Adults.

J Clin Exp Hepatol. 2025

[2]
Prevalence and risk factors of significant fibrosis in chronic hepatitis B patients with concurrent metabolic dysfunction-associated steatotic liver disease.

Ann Hepatol. 2024-9-19

[3]
A multisociety Delphi consensus statement on new fatty liver disease nomenclature.

J Hepatol. 2023-12

[4]
Noninvasive assessment of liver disease severity in patients with nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes.

Hepatology. 2023-7-1

[5]
A comparison of NAFLD and MAFLD diagnostic criteria in contemporary urban healthy adults in China: a cross-sectional study.

BMC Gastroenterol. 2022-11-19

[6]
Metabolic dysfunction-associated fatty liver disease and excessive alcohol consumption are both independent risk factors for mortality.

Hepatology. 2023-3-1

[7]
Immune mechanisms linking metabolic injury to inflammation and fibrosis in fatty liver disease - novel insights into cellular communication circuits.

J Hepatol. 2022-10

[8]
The transition from NAFLD to MAFLD: One size still does not fit all-Time for a tailored approach?

Hepatology. 2022-11

[9]
Are there outcome differences between NAFLD and metabolic-associated fatty liver disease?

Hepatology. 2022-11

[10]
Prevalence of advanced hepatic fibrosis and comorbidity in metabolic dysfunction-associated fatty liver disease in Korea.

Liver Int. 2022-7

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